Hsiao Hao-Ching, Gonzalez Kim L, Catanese Daniel J, Jordy Kristopher E, Matthews Kathleen S, Bondos Sarah E
Reynolds Medical Building, Department of Molecular and Cellular Medicine, Texas A&M Health Science Center, College Station, Texas, United States of America.
Department of Biochemistry and Cell Biology, Rice University, Houston, Texas, United States of America.
PLoS One. 2014 Oct 6;9(10):e108217. doi: 10.1371/journal.pone.0108217. eCollection 2014.
Interactions between structured proteins require a complementary topology and surface chemistry to form sufficient contacts for stable binding. However, approximately one third of protein interactions are estimated to involve intrinsically disordered regions of proteins. The dynamic nature of disordered regions before and, in some cases, after binding calls into question the role of partner topology in forming protein interactions. To understand how intrinsically disordered proteins identify the correct interacting partner proteins, we evaluated interactions formed by the Drosophila melanogaster Hox transcription factor Ultrabithorax (Ubx), which contains both structured and disordered regions. Ubx binding proteins are enriched in specific folds: 23 of its 39 partners include one of 7 folds, out of the 1195 folds recognized by SCOP. For the proteins harboring the two most populated folds, DNA-RNA binding 3-helical bundles and α-α superhelices, the regions of the partner proteins that exhibit these preferred folds are sufficient for Ubx binding. Three disorder-containing regions in Ubx are required to bind these partners. These regions are either alternatively spliced or multiply phosphorylated, providing a mechanism for cellular processes to regulate Ubx-partner interactions. Indeed, partner topology correlates with the ability of individual partner proteins to bind Ubx spliceoforms. Partners bind different disordered regions within Ubx to varying extents, creating the potential for competition between partners and cooperative binding by partners. The ability of partners to bind regions of Ubx that activate transcription and regulate DNA binding provides a mechanism for partners to modulate transcription regulation by Ubx, and suggests that one role of disorder in Ubx is to coordinate multiple molecular functions in response to tissue-specific cues.
结构化蛋白质之间的相互作用需要互补的拓扑结构和表面化学性质,以形成足够的接触来实现稳定结合。然而,据估计约三分之一的蛋白质相互作用涉及蛋白质的内在无序区域。无序区域在结合之前以及在某些情况下结合之后的动态性质,让人质疑伴侣拓扑结构在形成蛋白质相互作用中的作用。为了了解内在无序蛋白质如何识别正确的相互作用伴侣蛋白,我们评估了果蝇Hox转录因子超双胸(Ubx)形成的相互作用,Ubx既包含结构化区域也包含无序区域。Ubx结合蛋白富含特定的折叠结构:在其39个伴侣中,有23个包含SCOP识别的1195种折叠结构中的7种折叠结构之一。对于具有两种最常见折叠结构的蛋白质,即DNA-RNA结合三螺旋束和α-α超螺旋,伴侣蛋白中呈现这些偏好折叠结构的区域足以与Ubx结合。Ubx中三个含无序区域的部分是与这些伴侣结合所必需的。这些区域要么是可变剪接的,要么是多重磷酸化的,为细胞过程调节Ubx-伴侣相互作用提供了一种机制。实际上,伴侣拓扑结构与单个伴侣蛋白结合Ubx剪接异构体的能力相关。伴侣蛋白在不同程度上结合Ubx内不同的无序区域,从而产生了伴侣蛋白之间竞争以及伴侣蛋白协同结合的可能性。伴侣蛋白结合Ubx中激活转录和调节DNA结合区域的能力,为伴侣蛋白调节Ubx的转录调控提供了一种机制,并表明Ubx中无序区域的一个作用是响应组织特异性信号协调多种分子功能。